RXFP3
rxfp3 Gene: An Essential Player in Reproduction and Beyond
Description
The rxfp3 gene, also known as the relaxin family peptide receptor 3 gene, encodes a G protein-coupled receptor that binds to relaxin-3, a hormone involved in a wide range of physiological processes, particularly in reproduction. This gene is located on the X chromosome in humans and is composed of four exons and three introns.
Associated Diseases
Mutations or variations in the rxfp3 gene have been linked to several diseases and conditions, including:
- Infertility: In males, rxfp3 mutations can lead to impaired sperm production and motility, resulting in infertility.
- Preeclampsia: This serious pregnancy complication is associated with altered levels of relaxin-3 and rxfp3 expression.
- Cardiovascular disease: Studies suggest that rxfp3 may play a role in blood vessel regulation and inflammation, contributing to the development of cardiovascular diseases.
- Cancer: Some research indicates that rxfp3 expression may be involved in the growth and progression of certain cancers.
Did you Know ?
Approximately 1 in 100 women have a mutation or variation in the rxfp3 gene, making it a relatively common genetic condition.